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Mechanisms modulating foam cell formation in the arterial intima : exploring new therapeutic opportunities in atherosclerosis
La Chica Lhoëst, Maria Teresa (Institut de Recerca Sant Pau)
Martinez, A. (Institut de Recerca Sant Pau)
Claudi, Lene (Institut d'Investigacions Biomèdiques de Barcelona)
Garcia, E. (Institut de Recerca Sant Pau)
Benitez Amaro, Aleyda (Institut de Recerca Sant Pau)
Polishchuk, A. (Institut d'Investigacions Biomèdiques de Barcelona)
Piñero, J. (Universitat Pompeu Fabra)
Viladés Medel, David (Institut de Recerca Sant Pau)
Guerra Ramos, José María (Institut de Recerca Sant Pau)
Sanz, F. (Universitat Pompeu Fabra)
Rotllan, Noemi (Institut de Recerca Sant Pau)
Escolà-Gil, Joan Carles (Institut de Recerca Sant Pau)
Llorente-Cortés, Vicenta (Institut de Recerca Sant Pau)
Universitat Autònoma de Barcelona

Date: 2024
Abstract: In recent years, the role of macrophages as the primary cell type contributing to foam cell formation and atheroma plaque development has been widely acknowledged. However, it has been long recognized that diffuse intimal thickening (DIM), which precedes the formation of early fatty streaks in humans, primarily consists of lipid-loaded smooth muscle cells (SMCs) and their secreted proteoglycans. Recent studies have further supported the notion that SMCs constitute the majority of foam cells in advanced atherosclerotic plaques. Given that SMCs are a major component of the vascular wall, they serve as a significant source of microvesicles and exosomes, which have the potential to regulate the physiology of other vascular cells. Notably, more than half of the foam cells present in atherosclerotic lesions are of SMC origin. In this review, we describe several mechanisms underlying the formation of intimal foam-like cells in atherosclerotic plaques. Based on these mechanisms, we discuss novel therapeutic approaches that have been developed to regulate the generation of intimal foam-like cells. These innovative strategies hold promise for improving the management of atherosclerosis in the near future.
Grants: Instituto de Salud Carlos III FIS PI21/01523
Instituto de Salud Carlos III FI19/00205
Instituto de Salud Carlos III MV21/00060
Instituto de Salud Carlos III CB16/11/00276
Instituto de Salud Carlos III CB07/08/016
Ministerio de Economía y Competitividad RED2018-102799-T
Generalitat de Catalunya 2021 SGR 00834
Ministerio de Ciencia, Innovación y Universidades PID2022-137186OB-100
Agencia Estatal de Investigación RYC-201722879
Rights: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Language: Anglès
Document: Ressenya ; recerca ; Versió publicada
Subject: ApoA1 ; ApoB100 ; ApoC1 ; ApoE ; ApoJ ; Apolipoproteins ; Atherosclerosis ; Cardiovascular diseases ; Foam-like SMC ; Lipoproteins ; Peptidomimetics ; Reverse cholesterol transport ; Transcription factors
Published in: Frontiers in Cardiovascular Medicine, Vol. 11 (2024) , p. 1381520, ISSN 2297-055X

DOI: 10.3389/fcvm.2024.1381520
PMID: 38952543


11 p, 3.6 MB

The record appears in these collections:
Research literature > UAB research groups literature > Research Centres and Groups (research output) > Health sciences and biosciences > Institut de Recerca Sant Pau
Articles > Research articles
Articles > Published articles
Articles > Reviews

 Record created 2024-07-09, last modified 2024-07-18



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